FDA Inspection 662262 — The Metrix Company

The Metrix Company — FEI 1000117446

The FDA completed an inspection of The Metrix Company on April 22, 2010 in Dubuque, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dubuque, IA (United States)